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Sugar baker, p. (ed): Peritoneal Carcinomatosis: Principles of Management. 1995. ISBN 0-7923-3727-1.
Dickson, R.B., Lippman, M.E. (eds): Mammary Tumor Cell Cycle, Differentiation and Metastasis.
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Freireich, E.J, Kantarjian, H. (eds): Molecular Genetics and Therapy of Leukemia. 1995. ISBN 0-7923-3912-6.
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Tallman, M.S., Gordon, L.I. (eds): Diagnostic and Therapeutic Advances in Hematologic Malignancies.
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von Gunten, C.F. (ed.): Palliative Care and Rehabilitation of Cancer Patients. 1999. ISBN 0-7923-8525-X
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Sparano, J. A. (ed.): HP/& HTLV-I Associated Malignancies. 2001. ISBN 0-7923-7220-4.
Ettinger, D. S. (ed.): Thoracic Oncology. 2001. ISBN 0-7923-7248-4.
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Leong, S. P.L. (ed.): Atlas of Selective Sentinel Lymphadenectomy for Melanoma, Breast Cancer and
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Kirsch, M.; Black, P. McL. (ed.): Angiogenesis in Brain Tumors. 2003. ISBN 1-4020-7704-1.
Keller, E.T., Chung, L.W.K. (eds): The Biology of Skeletal Metastases. 2004. ISBN 1-4020-7749-1.
Kumar, R. (ed.): Molecular Targeting and Signal Transduction. 2004. ISBN 1-4020-7822-6.
Verweij, J., Pinedo, H.M. (eds): Targeting Treatment of Soft Tissue Sarcomas. 2004. ISBN 1-4020-7808-0.
Finn, W.G., Peterson, L.C. (eds.): Hematopathology in Oncology. 2004. ISBN 1-4020-7919-2.
Farid, N. (ed.): Molecular Basis of Thyroid Cancer. 2004. ISBN 1-4020-8106-5.
Khleif, S. (ed.): Tumor Immunology and Cancer Vaccines. 2004. ISBN 1-4020-8119-7.
Balducci, L., Extermann, M. (eds): Biological Basis of Geriatric Oncology. 2004. ISBN
Abrey, L.E., Chamberlain, M.C., Engelhard, H.H. (eds): Leptomeningeal Metastases. 2005. ISBN 0-387-24198-1
Platanias, L.C. (ed.): Cytokines and Cancer. 2005. ISBN 0-387-24360-7.
Leong, S. P.L., Kitagawa, Y., Kitajima, M. (eds): Selective Sentinel Lymphadenectomy for Human
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Small, Jr. W., Woloschak, G. (eds): Radiation Toxicity: A Practical Guide. 2005. ISBN 1-4020-8053-0.
Haefner, B., Dalgleish, A. (eds): The Link Between Inflammation and Cancer. 2006. ISBN 0-387-26282-2.
THE LINK BETWEEN
INFLAMMATION AND CANCER
Wounds that do not heal
edited by
ANGUS G. DALGLEISH, MD
Division of Oncology
St George's Hospital Medical School
London, UK
BURKHARD HAEFNER, PhD
Department of Oncology
Johnson & Johnson Pharmaceutical
Research and Development
BeersCy Belgium
Spri
ringer
Burkhard Haefner, PhD
Department of Oncology
Johnson and Johnson Pharmaceutical
Research and Development
Turnhoutseweg 30, Box 6423
2340 Beerse, Belgium
Angus G. Dalgleish, MD
Division of Oncology
St. George’s Hospital Medical School
Cranmer Terrace
London SW17 0RE, United Kingdom
THE LINK BETWEEN INFLAMMATION AND CANCER
Wounds that do not heal
Library of Congress Control Number: 2005934590
ISBN-10: 0-387-26282-2
ISBN-13: 978-0387-26282-6
e-ISBN-10: 0-387-26283-0
e-ISBN-13: 978-0387-26283-3
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¤ 2006 Springer Science+Business Media, Inc.
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SPIN 11053699
CONTENTS
Foreword
Angus G. Dalgleish and Burkhard Haefner
vii
Contributors
xi
1.
Inflammation and Cancer: The role of the immune
response and angiogenesis
Angus G. Dalgleish and Ken O'Byme
1
2.
Chronic Inflammation and Pathogenesis of GI and
Pancreatic Cancers
Lindsey N. Jackson and B. Mark Evers
39
3.
Cytokines, N F - K B , Microenvironment, Intestinal
Inflammation and Cancer
Amdt J. Schottelius and Harald Dinter
67
4.
Regulation of N F - K B Transcriptional Activity
Linda Vermeulen, Wim Vanden Berghe and Guy Haegeman
89
5.
The Role of Immune Cells in the Tumor
Microenvironment
Theresa L. Whiteside
103
6.
Tumor-Microenvironment Interactions: The SelectinSelectin Ligand Axis in Tumor-Endothelium Cross Talk
Isaac P. Witz
125
7.
CD95L/FasL and Trail in Tumour Surveillance and
Cancer Therapy
Harald Wajant
141
8.
Infection & Neoplastic Growth 101: The required reading
for microbial pathogens aspiring to cause cancer
Jessica Bertout and Andrei Thomas-Tikhonenko
167
9.
Cytokines as Mediators and Targets for Cancer Cachexia
Josep M, Argiles, Silvia Busquets and
Francisco J. Lopez-Soriano
199
10.
Targeting NF-KB in Anticancer Adjunctive
Chemotherapy
Burkhard Haefner
219
Index
247
FOREWORD
A link between inflammation and cancer has been established
many years ago, yet it is only recently that the potential significance
of this connection has become apparent. Although several examples of
chronic inflammatory conditions, often induced by persistent irritation
and/or infection, developing into cancer have been known for some
time, there has been a notable resistance to contemplate the possibility
that this association may apply in a causative way to other cancers.
Examples for such progression from chronic inflammation to cancer
are colon carcinoma developing with increased frequency in patients
with ulcerative colitis, and the increased incidence of bladder cancer
in patients suffering from chronic Schistosoma infection.
Inflammation and cancer have been recognized to be linked in another
context for many years, i.e., with regards to pathologies resembling
chronic lacerations or 'wounds that do not heal.' More recently, the
immunology of wound healing has given us clues as to the
mechanistic link between inflammation and cancer, in as much as
wounds and chronic inflammation turn off local cell-mediated
immune responses and switch on growth factor release as well the
growth of new blood vessels - angiogenesis. Both of these are
features of most types of tumours, which suggest that tumours may
require an immunologically shielded milieu and a growth factor-rich
environment.
The discovery that some cancers are associated with viral
infections and that these viruses only cause cancer in a small
percentage of infected individuals has served to highlight that these
'oncogenic' viruses are extremely 'mild' with regard to the time it
takes to induce cancer and that other factors must be involved.
Examples of these viruses include human papilloma viruses (HPV),
Epstein Barr Virus (EBV) and the two hepatitis viruses, HBV and
HCV. HPV causes cervical cancer in only a small percentage of
infected women, most of whom eventually become clear of infection.
Chronic infection with HPV would appear to be more likely in the
presence of additional infectious agents leading to established
infection and chronic cervicitis. EBV only rarely causes cancer in
Vlll
Western populations, but where it is clearly linked with cancers in a
causative sense, e.g. Burkitt's Lymphoma (BL) in Africa and
nasopharyngeal carcinoma (NPC) in China, there are other chronic cofactors involved. In the case of BL, there is a strong link to malaria
and with NPC, salted fish acting as an irritant/carcinogen is required.
However, HBV (and HCV) infection, over decades, will induce
chronic hepatitis which evolves into cirrhotic changes from which
hepatomas develop. Although co-factors may be involved, they do not
appear necessary. These examples emphasize that these are extremely
weak oncogenic viruses contained for years by an effective immune
response (the only clear link between EBV and tumours (lymphomas)
in the West are seen in immunosuppressed patients and the tumours
often resolve upon reversal of immunosuppression). The bottom line
is that all these viruses usually only cause malignant transformation
after many years of inflammatory infection.
The rapid growth in our understanding of molecular signaling
pathways in the past decades has taught us that some of these
regulatory cascades appear to be key to the development of cancer
from chronic inflammatory conditions. Pivotal among these signaling
circuits appears to be the NF-KB pathway, crucial for the regulation of
immune and inflammatory responses, and linked to non-inflammatory
core pathways in oncogenesis, such as the p53 pathway. A major
focus of this book, therefore, is the NF-KB pathway as well as the
interaction between the tumour and its microenvironment involving
the immune response, apoptotic pathways, cytokines and the selectins.
In this volume we have tried to highlight the complexity of these
processes, yet at the same time show just how fundamental the basic
link is. Inevitably this means looking at the same scene from different
angles, and hence, there is some degree of overlap. However, the
detail is so impressive that we feel this helps enforce the clarity of the
overall picture, which only goes to raise the question: 'Why has the
link been denied for so long?' The major impact of this book,
however, should be to emphasize the obvious dramatic therapeutic
and preventative implications. Chronic viral infections, for example,
can be vaccinated against. For instance, the widespread availability of
a HBV vaccine for several decades has greatly reduced the incidence
of hepatoma and, as such, can claim to be the first effective
preventative cancer vaccine. The common 'non-infection'-related
tumours such as colon, lung, breast, and prostate cancer, may be
'preventable' by regular administration of anti-inflammatories such as
IX
aspirin. More specific drugs may be derived from studies included in
this book which will lead to more effective preventative strategies as
well as treatments. The link between an inflammatory environment
and more rapid progression has been recognized for a number of
tumours, including breast cancer, clearly suggesting that antiinflammatory agents may have a major role in therapy. Unfortunately,
several studies using the new COX-2 inhibitors have had to be halted
because of the association with increased heart attack risk. Aspirin of
course is a COX inhibitor which protects against heart attacks and is
an obvious candidate. Unfortunately, gastritis and increased gastric
bleeding tendency have reduced enthusiasm for such studies even
though aspirin has been reported to be preventative for a number of
solid tumours, including breast cancer as well as colorectal cancer.
Clearly, there still is ptenty of scope for the development of improved
anti-inflammatory drugs which can be used in cancer prevention as
well as treatment.
The recognition of the link with chronic inflammation allows
for new ways of understanding how cancers progress and how
different types of cancer can show similar responsiveness to drug
treatment, which is already being seen for Avastin, a monoclonal
antibody which targets vascular endothelial growth factor and is active
in disparate tumour types. Another example of how this approach can
influence cancer treatment is Revlimid, a Thalidomide analogue
developed by Celgene. It was selected for its anti-TNF and thus antiinflammatory activity but was found to also have strong antiangiogenic properties and to stimulate the cell-mediated immune
response. This compound may thus deliver an ideal three-way blow to
tumours and has recently been shown to be highly active against
multiple myeloma. It would be surprising if it did not act against other
tumour types as well. Thus, we feel confident in proclaiming that this
book does not merely cover a speculative theory, but rather the basis
for a therapeutical revolution in the treatment of cancer.
Angus G, Dalgleish, MD
Burkhard Haefner, PhD
CONTRIBUTORS
Josep M, Argiles, PhD, Professor, Department of Biochemistry and
Molecular Biology, Faculty of Biology, University of Barcelona,
Barcelona, Spain
Jessica Bertout, Center for Research on Reproduction and Women's
Health, University of Pennsylvania Medical Center, Philadelphia, PA
Silvia Busquets, MD, Department of Biochemistry and Molecular
Biology, Faculty of Biology, University of Barcelona, Barcelona,
Spain
Angus G. Dalgleish, MD, Professor, Division of Oncology,
St. George's Hospital Medical School, London, UK
Harald Dinter, PhD, Scientific Director of Oncology Research,
Berlex Biosciences, Richmond, CA
B. Mark Evers, MD, Professor and Robertson-Poth Distinguished
Chair in General Surgery, Department of Surgery and Director,
The Sealy Center for Cancer Cell Biology, The University of Texas
Medical Branch, Galveston, TX
Burkhard Haefner, PhD, Department of Oncology, Johnson &
Johnson Pharmaceutical Research and Development, Beerse, Belgium
Guy Haegeman, PhD, Professor, Laboratory for Eukaryotic Gene
Expression and Signal Transduction (LEGEST), Department of
Molecular Biology, Ghent University, Gent, Belgium
Lindsey N. Jacksoriy MD, Department of Surgery, The University
of Texas Medical Branch, Galveston, TX
Xll
Francisco J, Lopez-Soriano, MD, Department of Biochemistry and
Molecular Biology, Faculty of Biology, University of Barcelona,
Barcelona, Spain
Ken O'Byrne, MD, Consultant and Clinical Lecturer in Medical
Oncology, St James's Hospital and Trinity College, Dublin Ireland
Arndt J. Schottelius, MD, Director, Non-Clinical Immunology Drug
Development, Development Sciences, Genentech, Inc., South San
Francisco, CA
Andrei Thomas-Tikhonenko, PhD, Associate Professor, Department
of Pathobiology, University of Pennsylvania, Philadelphia, PA
Wim Vanden Berghe, PhD, Laboratory for Eukaryotic Gene
Expression and Signal Transduction (LEGEST), Department of
Molecular Biology, Ghent University, Gent, Belgium
Linda Vermeulen, PhD, Laboratory for Eukaryotic Gene Expression
and Signal Transduction (LEGEST), Department of Molecular
Biology, Ghent University, Gent, Belgium
Harald Wajant, PhD, Professor, Department of Molecular Internal
Medicine, Medical Clinic and Polyclinic II, University of Wuerzburg,
Wuerzburg, Germany
Theresa L Whiteside, PhD, Professor, University of Pittsburgh Cancer
Institute, Hillman Cancer Center, Pittsburgh, PA
Issac P. Witz, PhD, Professor, Department of Cell Research and
Immunology, The George S. Wise Faculty of Life Sciences,
Tel Aviv University, Tel Aviv, Israel
Chapter 1
INFLAMMATION AND CANCER:
The role of the immune response and angiogenesis
Angus G. Dalgleish^ and Ken O'Byrne^
^Division of Oncology, St. George's Hospital Medical School, London, UK
^Medical Oncology, St James's Hospital and Trinity College, Dublin, Ireland
Abstract:
The link with chronic inflammation and cancer has been recognized for certain
cancers for several decades. However, only recently has the biology of chronic
inflammation begun to be understood, to the point that it may play a major role
in tumour development. The biology of chronic inflammation has many
similarities with that of wound healing. In particular, local cell mediated
immunity is attenuated and angiogenesis is increased along with other growth
factors. When present long term, this provides the ideal environment for
mutated cells to be nurtured and escape immune surveillance. It is of note that
this process still appears to take two or three decades, as witnessed by the
close association between chronic ulcerative colitis and colon cancer as well as
chronic hepatitis and hepatocellular carcinoma. Closer study of the
inflammatory pathways show the close interaction with apoptosis and antiapoptotic pathways, as well as the main tumour suppressor genes, such as p53,
as well as a number of growth factors, such as the insulin-like growth factor. A
full study of these processes reveals that there are key molecules in these
pathways which may provide therapeutic as well as anti-inflammatory targets.
2
1.
Chapter 1
INTRODUCTION
The association between chronic inflammation and cancer is not new.
However, the previously recognized associations had limited practical
implications and it is only the relatively recent understanding of molecular
mechanisms of cancer and the interaction of the immune system and
angiogenesis that have led to the potential for targeted intervention to both
prevent and treat a number of different cancers.
It was recognized in the nineteenth century that certain cancers were due
to chronic irritation, notably the scrotal cancer of chimney sweeps where the
irritant was the coal dust and male breast cancer associated with chronic
irritation by braces. It was Virchow in 1863 who wrote about the
possibilities of cancers arising from sites of chronic inflammation, noting
that cancers are similar to wounds that failed to heal. The striking similarities
between wound healing and tumour stroma have been reviewed more
recently by Dvorak. (Dvorak 1986) Other chronic inflammatory conditions
that are recognized as being associated with an increased risk of cancer
include schistosomiasis (bladder) and ulcerative colitis (colon).
2.
INFECTIOUS CAUSES
The relatively recent realization that many chronic bacterial and viral
infections are also associated with tumour formation provides the most
compelling examples. In addition to schistosomiasis and bladder cancer, the
more recently discovered Helicobacter pylori, originally associated with
chronic gastritis, is now recognized as a causative agent for gastric
adenocarcinoma and gastric mucosal-associated lymphoid tissue lymphomas
(Williams and Pounder, 1999).
2.1
Virus association
Perhaps the strongest association between chronic infection and the
development of cancer is that between chronic viral infections and tumour
induction. (Dalgleish, 1991). The best examples are those of chronic
hepatitis B and hepatitis C virus infection, both of which cause chronic
hepatitis from which primary liver cancers evolve, often decades later.
Similarly, chronic human papilloma virus infection is clearly associated with
inflammatory changes in the cervix leading to cervical cancer and cancers of
the perineal region. Epstein Barr Virus (EBV), which exists in a dormant
1. Inflammation and Cancer
3
state in the vast majority of the Western population, is able to cause Burkitt's
lymphoma in Africa, where the additional stimulus is chronic immune
activation, probably by malaria. Similarly, it is associated with
nasopharyngeal carcinoma, particularly in the Far East where chronic
irritation/inflammation/immune activation by salted fish stimulates EBV
replication leading to these unusual tumours. EBV is largely asymptomatic
but is clearly able to cause lymphomas, particularly in immunosuppressed
patients, such as post transplant patients or acquired immune deficiency
syndrome (AE)S) patients.
The most recent example of a virus causing a tumour is the discovery of
the new herpes sarcoma virus or human herpesvirus 8 (HHV-8), which is the
causative agent of Kaposi's sarcoma (Brooks et aL, 1997). There is a strong
association with HIV and this cancer may undergo spontaneous resolution
with treatment leading to a reduction of HIV load. HIV is associated with
chronic immune activation, which is reduced when the viral load is lowered.
2.2
The requirement for chronic inflammation
Although the viruses above have well described oncogenic properties,
they rarely cause disease in the absence of chronic immune activation or
inflammation. The fact that chronic irritation/inflammation does not need to
be caused by an infectious agent in order to increase the propensity for
cancer to develop is clearly shown by tobacco-related cancers. Lung cancer,
for instance, is clearly associated with smoking and it is dependent on the
amount smoked (packs per day) as well as the number of years smoked.
Many of the patients suffer from chronic bronchitis for a number of years
and even in those patients who do not have overt bronchitis, histology of non
macroscopically tumour-free bronchi show chronic inflammatory changes.
Other chronic irritants also lead to inflammation and subsequent tumours,
such as asbestos in mesothelioma. Inappropriate enzymatic exposure can
also result in chronic inflammation. For example, reflux esophagitis and
Barratt's esophagitis are both associated with the development of esophageal
adenocarcinoma. For a full list of associations of cancer or recognized
associations of cancer and chronic infection/irritation/inflammation see
Table 1.
The association between chronic inflammation and tumour formation
strongly suggests that sites of chronic inflammation are ideal
microenvironments for cancer to evolve (Table 1). Here, the similarity with
wound healing is pertinent as in wounds, cell-mediated immunity is
suppressed, presumably to prevent breaking of tolerance of "self tissue as it
is being repaired. The second component is the induction of angiogenesis,
being new blood vessel formation which in itself is associated with increased
Chapter 1
Table 1. Relationship) between known causes of Chronic
Cancer
Causative
inflammatory stimulus
EBV
Burkitts Lymphoma (BL)
Nasopharyngeal (NFL)
Post transplant lymphoma
Immunosuppression associated
lymphoma
NHL
Breast cancer
HBV/HCV
Viruses induce hepatitis followed
by cirrhosis (angiogenesis)
followed by oncogenic
transformation - hepatic cancer
HPV
Cervix/anal/perineum/?upper
aerodigestive track
HHV-8
Kaposi's Sarcoma
HIV
•
•
HTVL-1
1
1
1
Helicobacter
pylori
Schistosomiasis
Tobacco smoke
Nicotine
Infections
Asbestos
Ulcerative colitis
Crohn's
? bile salts
Reflux
+?
Prostatitis
?cause
Chronic
pancreatis
?cause
UV light
Chronic tar/soot
irritation
Lymphoma (EBV driven)
Kaposi's Sarcoma (HHV-8
driven)
•
Cervix (HPV driven)
•
(HIV is not oncogenic directly
in contrast to the above)
T-cell lymphomas and
•
leukaemia
•
Stomach cancer
•
Lymphoma of gut (MALT)
Bladder
Lung cancer
Inflammation and Cancer
Mechanism of action and
1
precursor states
Associated with chromic
1
immune activation such as
malaria in BL and smoked food
in NPC
Immune suppression post
transplantation
Aflatoxin may enhance the
degree of inflammation
May require extra exogenous
causative agent of cervicitis to
progress, e.g. chlymidia, and/or
immunosuppression
Only in presence of
immunosuppression due to age
(mild) or HIV infection
(aggressive) which causes
marked immune activation
HIV induces
immunosuppression as well as
chronic immune activation
which appears dependant on the
immunogenetics of host
Causes chronic T-cell activation
Gastritis/ulcers
Chronic cystitis
Chronic bronchitis
Inflammation of tunica medica
Prostate cancer
Asbestos, fibrotic, plaques
Causes of inflammatory bowel
disease including polyps and
adenomas
Oesophagitis/obesity/tobacco/
nicotine
?infectious cause
Pancreatic cancer
Causative agent unclear
Melanoma
Skin inflammation and
immunosuppression
Common in chimney sweeps in
Victorian era
Mesothelioma
Colorectal cancer
Oesophageal cancer
Scrotum
7. Inflammation and Cancer
5
amounts of growth factors. If continued indefinitely, as in chronic
inflammation, this environment would be ideal for cancer to develop. It is
broadly recognized that cancer is a sequence of stochastic events involving
permanent activation of oncogene pathways and deletion of tumour
suppressor genes and their pathways. On average, six such events are
required to occur for cancer to develop. It has been shown that single
mutations in oncogenes can be recognized by cytotoxic T lymphocytes
suggesting that in the absence of suppression of the immune system, a cell
developing such a mutation would induce an immune response against this
new epitope and the cell would be killed. In a background of chronic
inflammation, immune induction does not occur and the cell is able to
survive long enough to develop the next random event. When the tumour
does start to develop, it has an environment full of growth factors and the
ability to establish new vasculature.
The most important impact of the association between chronic
inflammation and cancer is that treatment of chronic inflammation should
lead to a lower incidence of cancer. This is one of the most convincing
aspects of the association as there are numerous studies showing that the
daily use of anti-inflammatories, such as aspirin, other NSABDS, and
cyclooxygenase (COX)-2 inhibitors, are able to reduce the incidence of
colorectal cancer by up to half. In addition, the incidence of other solid
tumours are also reduced by a significant amount (Harris et aL, 2005).
3.
CANCER AND THE IMMUNE RESPONSE
T cells produce (at least) two major cytokine patterns. The first is
generated by Th-1 cells, which produce interleukin (IL)-2, interferon (DFN)y, and IL-12 and affect the cell mediated immune (CMI) response, and the
second by Th-2 cells, which release IL-4, IL-5, IL-6, and BL-IO and affect
the hormonal response (HIR). This discovery, initially in mice but later also
in humans, has had a major impact on understanding the complex changes
and interactions between an infectious agent and the immune system
(Mosman and Coffman, 1989). Th-1 cytokines are required for a strong CMI
response and are decreased in many chronic infectious diseases, including
ADDS, tuberculosis (TB), and many tropical infections. In what might appear
a compensatory response, Th-2 cytokines are associated with humoral
immunity (HI) and often increase as is the case in diseases where CMI is
suppressed, e.g., ADDS and tuberculosis.
Many malignancies are associated with some degree of suppression of
CMI responses (Lee et al 1997; Maraveyas et al, 2000; Pettit et al., 2000).
Cancers use a wide variety of methods to evade an immune response
including downregulation of molecules of the major histocompatibility
6
Chapter 1
complex (MHC, HLA in humans) and upregulation of ligands that kill
engaging killer T-cells, i.e. CD95L and DC178. The production of
immunosuppressive cytokines by tumours, such as TGPp and IL-10 could
account for much of the inhibition of CMI (Doherty et al, 1994; Ganss and
Hanahan, 1998; Garrido et al, 1993; Gorter and Meri, 1999; Melief and
Kast, 1991; Strand and Galle, 1998; Pettit et al, 2000).
The suppression of local CMI responses has been reported in a number of
studies evaluating inflammatory cellular infiltrates in tumours from patients
with malignant cancers including non-small cell lung cancer (NSCLC), head
and neck, oesophagus, breast and genitourinary cancers, lymphomas and
sarcomas (Asselin-Paturel et al, 1998; O'Sullivan et a/., 1996; Hildesheim
et al, 1997; Lee et al, 1997; Aziz et al, 1998; O'Hara et al, 1998) as well
as carcinoma in situ including Barrett's oesophagus and cervical
intraepiithelial neoplasia (CIN) (Hildesheim, et al 1997; Oka, et al. 1992;
Sonnex, 1998). Systemic immunosuppression can be documented by looking
at intracellular cytokine production following stimulation of lymphocytes in
vitro and has been shown in several cancer types including melanoma and
colorectal cancer (Maraveyas et al, 1999; Heriot et al, 2000). The presence
of a dominant Th-2 immune response in potentially curable tumours, such as
lymphomas, is associated with a fatal outcome (Lee et al, 1997). Absent or
reduced delayed hypersensitivity reactions to common T-cell recall antigens
are a manifestation of CMI, These responses are either reduced or absent in
many pre-malignant and malignant tumours including CIN, Hodgkin's
disease, gastric carcinoma, small cell lung cancer, and malignant melanoma
(Roses et al, 1979; Lang et al, 1980; Johnston-Early et al, 1983;
Richtsmeier and Eisele, 1986; Cainzos, 1989; Hopfl et al 2000).
T-cell anergy is commonly seen in malignant disease. A number of
processes may be responsible for this. T-cells from cancer patients have
abnormalities in their signal transduction pathways. The T-cell receptor
(TCR)-a(3 or -yS chains bind the peptide ligand while, in turn, the TCR is
coupled to intracellular signal transduction components by TCR-^ subunits.
The TCR-associated signalling molecule CD3 is made up of a number of
components which stabilize surface expression of the TCR and are essential
for interaction with MHC-antigen complexes. The T-cell alterations found in
in vivo models of malignant disease include complete absence of CD3-^
which is replaced by the Fc ey-chain and a reduction in the ability of T
lymphocytes to produce the Th-1 cytokines IL-2 and IFN-y (Mizoguchi et
al, 1992; Salvadori et al, 1994; Zea et al, 1995).
In malignant mesothelioma, the relative CD5, CDyand CD^ mRNA
levels expressed by tumour infiltrating lymphocytes (TILs) decrease. In
addition, transforming growth factor-P (TGPP), a potent tumour cell growth
and immunosuppressive factor, is produced. (A feature which is not limited
7. Inflammation and Cancer
7
to mesothelioma.) In this disease, however, the suppression of CD3 subunit
expression with resultant functional impairment of TDLs is reversed in vivo
by inducing TGpp antisense RNA. This indicates that TILs are deactivated
by tumour-associated immunosuppressive factors upon infiltration of the
tumour microenvironment (Jarnicki et al, 1996).
COX enzymes are responsible for the synthesis of prostaglandins, the
precise prostaglandin synthesized depending on the prostaglandin synthase
enzyme present in the cell. COX-2, the inducible form of the enzyme, is
constitutively expressed in virtually all premalignant and malignant cancers,
including colorectal, upper gastrointestinal tract, pancreatic, head and neck,
lung and breast cancers (Murata et al, 1999; Koshiba et al, 1999; Mestre et
aL, 1999; Molina et al, 1999; Wolff et aL, 1998; Huang et al, 1998; Taketo,
1998; Tsujii et al, 1997; Uotila, 1996; Vainio and Morgan, 1998; Vane et
ai, 1998). More recently, COX-2 expression has been shown to correlate
with local chronic inflammation and tumour neovascularisation in human
prostate cancer (Wang, et al, 2005). It is particularly associated with
prostaglandin E2 (PGE2). On binding to its receptor on T-cells, PGE2
induces cyclic adenosine monophosphate (cAMP) which inhibits the
proliferation of Th-1/CMI-associated CD4"*^ lymphocytes while stimulating
the proliferation of Th-2 CD4"*^ lymphocytes resulting in avoidance of
immunesurveillance. The importance of the Th-l/CMI response in both
tumour regression and rejection underscores the significance of these
changes. Tumour-specific cytotoxic T-cells represent a major effector arm of
theTh-1/CMI response as demonstrated by studies of adoptive T-cell transfer
(Greenberg, 1991; Papadopoulos et al, 1994; Rooney et al, 1995).
However, the presence of such effector cells is only seen in a small minority
of cases in the setting of tumour progression. Both Th-1 and Th-2 cytokine
gene transduction experiments in animal tumour cell lines have resulted in
CMI responses capable of inhibiting a subsequent challenge with parental
tumour cells. Moreover, in order to induce established tumour regression,
Th-1 cytokine secreting effector cells are required (Forni and Foa, 1996),
and where tumour rejection occurs, the induction of tumour-specific CMI
responses is generally seen. Collectively these findings indicate that tumour
growth either fails to stimulate an effective CMI response or evades
immunesurveillance at least in part through inhibition of TIL CMI functions
both locally and systemically (Browning and Bodmer, 1992; Jarnicki et al,
1996).
Malignant melanoma is a highly metastatic cancer of the melatoninproducing cells of the skin and is notoriously resistant to classical treatments
such as chemotherapy and radiotherapy. Employing the same fluorescenceactivated cell sorting (FACS) techniques used to detect intracellular
cytokines in AIDS patients, a significant reduction in Th-1 cytokine
8
Chapter 1
production can be found in these patients (Maraveyas et al, 1999). For many
years, however, it has been recognised that this cancer is sensitive to a
variety of immunology-based therapies which act by boosting CMI
responses. Skin lesions often disappear following direct intralesional
administration of Bacillus Calmette-Guerin (BCG) vaccine. Similar
responses have been seen with cell-based vaccines or lysates, melanoma
specific peptides, either given alone or pulsed onto dendritic cells.
Successful treatment with immunotherapy, resulting in either stable disease
or an objective tumour response has been found to be associated with a
switch from a Th-2/HI dominant profile to a Th-l/CMI dominant one
(Grange et aL, 1995; Sredni et al, 1996; Hu et al, 1998; Hrouda et aL,
1998; Dalgleish, 1999).
The impact of a reduced CMI response being induced by a tumour is
illustrated by colorectal cancer in which even in patients with early small
volume (Duke's A and B) tumours, a reduction in systemic Th-1-like
responses is seen compared to age- and sex-matched controls without
disease (Heriot et aL, 2000). In the latter case, the observation that these
responses return to normal following surgery strongly supports the deduction
that it is the tumour that causes the reduction in CMI responses. More
recently, the same patients have been reanalysed and the level of Th-1
responses have been found to correlate with survival irrespective of
subsequent treatment (Charles Evans and co-workers, unpublished data).
In NSCLC malignant pleural effusions, the majority of lymphocytes are
T-cells with a Th-2 phenotype whilst less than 1% are natural killer cells.
Following Th-1 cytokine therapy with IL-2 and IL-12, the T-helper
lymphocytes shift to a Th-1 phenotype. The specific anti-tumour cytotoxic
property of these T-lymphocytes can be restored by the use of IL-2 treatment
and TCR-CD3 engagement. IL-2 and IL-12 act synergistically in this setting
(Chen et aL, 1998; Chen et aL, 1997b).
Gene knockout experiments have provided the most conclusive evidence
for an association between deficient Th-1 responses and a predisposition to
cancer. An increased incidence of solid tumours is seen in IFN-y, IFN-y
receptor or signal transducer and activator of transcription (STAT) 1 (a
component of the IFN signalling pathway) knockout mice (Chen et aL, 1998;
Kaplan et aL, 1998). Therefore CMI suppression may provide the ideal
environment for cancer cells to develop and grow. A single mutation in an
oncogene would probably be identified by a cytotoxic T lymphocyte in a
normal environment but cells carrying such a mutation are able to survive in
a privileged, depressed CMI immune response site. As a result, the mutation
may persist leaving the cells' DNA primed for another stochastic event to
occur, such as a p53 mutation.
1. Inflammation and Cancer
9
As the neoplastic lesion grows, it becomes progressively hypoxic.
Hypoxia is associated with suppression of CMI responses (Lee et al, 1998;
Sairam et al, 1998) which in turn would allow escape of the malignant
process from immunesurveillance. Collectively these findings indicate that
effective reversion of immune tolerance may have a role to play not only in
the treatment of established malignant disease but also in chemoprevention.
Exposure to a foreign antigen results in upregulation of the non-specific
pro-inflammatory cytokines IL-la and P and the Th-1 cytokines in
inflammatory cells. COX-1 and -2 are among the most important enzymes in
the regulation of the immune response and play a key role in angiogenesis,
the inhibition of apoptosis, cell proliferation and motility. COX-1 is
constitutively expressed by many cells. In contrast COX-2 is produced by
epithelial, mesenchymal and inflammatory cells following exposure to proinflammatory cytokines (Taketo, 1998; Uotila, 1996; Vane et al, 1998),
which are induced by infective agents and environmental factors known to
be associated with the development of malignant disease including
Helicobacter pylori infection (Sawaoka et al, 1998a), nicotine (Schror et al,
1998), and tobacco-specific nitrosamine 4-(methylnitrosamino)-4-(3pyridyl)-l-butanone (NNK) (El-Bayoumy et al, 1999). Overexpression of
COX-2 is sufficient to induce tumorigenesis in the mammary glands of
transgenic mice derived using the murine mammary tumour virus promoter
(Liu et al, 2001). Th2 cytokines, such as IL-4 and BL-IO, which can inhibit
the synthesis of Th-1 cytokines by CD4^ T-helper lymphocytes, are
produced in COX-2 expressing environments. These Th-2 cytokines not only
downregulate both pro-inflammatory/Th-1 cytokines but also COX-2
expression itself (Delia Bella et al,1997; Subbaramaiah et al, 1997; Uotila,
1996; Vane et al, 1998) (Fig. 1). Chronic antigen exposure may drive a
continuous cycle in which induced pro-inflammatory and Th-1 cytokines
upregulate COX-2 leading to chronic HI/Th-2 cytokine production and
subsequent impairment of the CMI response. In predisposed individuals, this
cycle may eventually lead to a predominant HI response environment. The
importance of pro-inflammatory cytokines driving the HI response is
underpinned by the observation that TNF-deficient mice are resistant to skin
carcinogenesis (Moore et al, 1999).
The results of these studies consistently demonstrate that not only is
cancer itself associated with a shift from a Th-1 to a Th-2 dominant
phenotype but that conditions predisposing to malignant disease likewise
induce similar changes. This suggests that in many cases, the immune
response shift precedes the development of the neoplastic process and may
play a key role in carcinogenesis.
10
Chapter 1
'Antigenic'
Carcinogenic
Stimuli
Physical
Viral
Cigarette smoke
Asbestos
Sunlight (UV-B)
HIV HHV8
HPV SV40
HBV HCV
EBV
Chemical
Dihydroxy bile salts
NNK
COX-2
PGE2
i Thl and t Th2
cytokine synthesis
t angiogenic growth
factor expression
e.g. VEGF, TGF-P
J^Apoptosis
tAngiogenesis
iCell Mediated
Immunity
Figure 1. Exposure to carcinogenic stimuli results in upregulation of cell survival factors in affected
cells including cyclooxygenase (C0X)-2. COX-2 plays a key role in the conversion of arachidonic
acid to prostaglandins including PGE2. PGE2 downregulates the synthesis of Thl cytokines and
upregulates Th-2 cytokines in inflammatory and/or affected epithelial, mesenchymal or
haematopoietic cells resulting in suppressed cell mediated immune responses (CMI), increased
angiogenesis and inhibition of apoptosis. In an acute exposure situation the feedback between the
initial pro-inflammatory response and the anti-inflammatory Th2 cytokines is self-limiting.
However in the case of cancer associated chronic immune activation conditions sustained exposure
to the antigen/chemical drives the cycle continuously resulting in a sustained pre-dominant Th2
immune response, angiogenesis and inhibition of apoptosis facilitating the development of cancer
in a pre-disposed individual.
4.
INITIAL INFLAMMATION RESPONSE:
KILL OR CURE
The difference between a pro-inflammatory response to an antigen or
irritant and the type of immune response established is crucial as to whether
the cancer is fed by inflammation or is rejected by it. There are numerous
factors which can determine whether an immune response favours cancer
progression or its elimination. There are several studies showing that tumour
infiltrating lymphocytes are a good prognostic factor. Indeed, reculturing
these lymphocytes and expanding them ex vivo before re-infusion with IL-2
L Inflammation and Cancer
11
was reported as being capable of inducing clinical responses (Rosenberg et
al, 1986). However, it is now apparent that non-infiltrating immune cells are
exhibiting anti-tumour activity. Tumour-associated macrophages (TAMs)
have been shown to correlate with vessel density in a number of
malignancies and the associated expression of epidermal growth factor
(EGF) and EGF receptor (EGFR) in cancer cells. This is associated with
reduced patient survival. Co-culture of cancer cells with macrophages can
actually enhance cancer cell invasive potential and matrix degrading activity
and upregulate pro-tumorigenic genes. Chen et al have shown that this
activity can be reduced with anti-inflammatory drugs, including Thalidomide
(Chen et al, 2005). Whether the macrophages have a positive or negative
effect on tumour growth clearly depends on the tumour microenvironment
and the stroma involved. Indeed, different results reported in the literature
would appear to be dependent on whether the macrophages are
predominantly in the tumour islets or in the stroma. Thus, it would appear
that macrophages predominantly in the stroma are pro-tumorigenic, whereas
macrophages predominant in the tumour islet are associated with a
significant survival time. Indeed, Tomas Walsh and colleagues (personal
communication) have noted that patients with a high islet macrophage
density but incomplete resection have an overall longer survival than
patients with low islet macrophage density but complete resection.
What determines the result of this interaction is unclear but would appear
to involve chemokines and their receptors as most cancers express an
extensive network of these. Tumour-associated chemokines are thought to
control leukocyte infiltration into the tumour, the immune response against it,
the regulation of angiogenesis and the control of metastatic spread.
Chemokines can influence the distribution of the immune response, including
lymphocytes, monocytes/macrophages and pre-dendritic cells. They are also
able to promote angiogenesis and may also contribute directly to the
transformation of cells by acting as growth and survival factors. Moreover,
they are crucial to the spread of cells. Indeed, in mouse models, the level of
expressed tumour-derived chemokines determines whether macrophage
infiltration is pro-tumorigenic or capable of destroying tumour cells.
Manipulating chemokine levels and their receptors clearly could have a major
role in the treatment of cancer. In order to reject a tumour, an acute, as
opposed to a chronic inflammatory state needs to be introduced. Here, it is
clear that the interplay between innate and adaptive immunity and, in
particular, the interactions between NK and dendritic cells are of vital
importance for effective tumour control (de Visser and Coussens, 2005). The
importance of the immune response in controlling the development of cancer
can only be fully appreciated when considering the numerous methods
12
Chapter 1
employed by tumours to escape immune control (reviewed by Igney and
Krammer, 2005).
5.
THE INTER-RELATIONSIP BETWEEN THE
IMMUNE RESPONSE AND ANGIOGENESIS
The relationship between the immune response and angiogenesis
(O'Byrne et aL, 2000a) is important in its own right with regard to fostering
tumour growth. Angiogenesis, the formation of a new blood supply from an
existing vasculature, is necessary for the development of early neoplastic
lesions and the growth of invasive and metastatic disease. This process
occurs in all tumours and is under the regulation of pro-angiogenic factors
including Th-2 cytokines such as IL-6 and vascular endothelial growth factor
(VEGF). The intensity of the angiogenic process, as assessed by micro vessel
counting methods, correlates with primary tumour growth, invasiveness, and
metastatic spread of the disease (Folkman, 1995; O'Byrne et al, 2000b).
Furthermore, there is a strong correlation between tumour cell expression of
angiogenic growth factors, such as VEGF and angiogenesis, and patient
outcome (O'Byrne et al, 2000b).
Recent research indicates that normal physiological processes which
require angiogenesis, such as ovulation, implantation into the ovary and
wound healing, occur in a Hl-predominant environment (Folkman, 1995;
Richards et ai, 1995; Kodelja et al, 1997; Piccini et al, 1998; Schaffer and
Barbul, 1998; Singer and Clark, 1999). Hl-stimulated macrophages induce
endothelial cell proliferation 3 to 3.5 times more than CMI stimulated
macrophages in coculture experiments (Kodelja et al, 1997). These findings
are supported by work in IL-6 knockout mice where the capacity to heal
wounds and regenerate normal hepatic tissue, both processes which require
angiogenesis, is impaired (Gallucci et al. 2000; Wallenius et aL, 2000). In
contrast to the upregulated HI immune response seen, CMI responses are
suppressed during ovulation, implantation, and wound healing. This prevents
rejection of sperm and embryo, and presentation of damaged tissues to the
immune system as non-self, which might induce an autoimmune response to
healing or healed tissues (Richards et al, 1995; Piccini et al, 1998; Schaffer
and Barbul, 1998; Singer and Clark, 1999). In contrast to HI immune
response-induced angiogenesis, CMI immune responses tend to inhibit
angiogenesis (Watanabe et al, 1997). B lymphocytes, which are
synonomous with HI have been shown to be vital in promoting chronic
inflammation-dependent de novo carcinogenesis (de Visser et al, 2005).
Unlike normal physiological processes, the factors that suppress CMI and
switch on angiogenesis persist in many established chronic
infectious/inflammatory states, particularly conditions associated with the
L Inflammation and Cancer
13
subsequent development of malignant disease (Fig. 2). These include chronic
viral infections (see below), asbestos (Bielefeldt-Ohmann et al, 1996) and
cigarette smoke (Mayne et al, 1999). Chronic exposure to cigarette smoke
leads to chronic obstructive pulmonary disease (COPD) in predisposed
individuals. COPD is an independent predictor for the development of lung
cancer (Mayne et al, 1999). In keeping with this, inflamed lung mucosa has
increased vascularity compared with uninflamed mucosa (Fisseler-Eckhoff
et al, 1996). Furthermore, bronchial dysplasia and carcinoma in situ,
precursors to the development of malignant disease, have increased
vascularity compared to normal bronchial epithelium (Fontanini et al, 1996;
Fisseler-Eckhoff et al., 1996). Using fluoroscent bronchoscopy, angiogenic
squamous dysplastic lesions have been identified in 34 percent of high risk
smokers without carcinomas and in 60 percent of patients with squamous
cell lung carcinoma (Keith et al, 2000). Cigarettes contain a number of
factors, including nicotine, which may predispose to the development of
malignant disease. Nicotine induces angiogenesis and reduces CMI which
would facilitate the survival and proliferation of a cell transformed by
carcinogens such as NNK (Heeschen et al, 2001).
Angiogenic
environment
Angiogenesis
Carcinogens
Chronic
Inflammation
Genetic
Mutations
Initiation-^ Promotion-^ / Tumour
i(^"i
L Growth
Immunosuppression
Suppressed
CMI
Predominant
HI
Suppression
CMI
Predominant
HI
Figure 2. The inflammatory environment resulting in angiogenesis and growth factors, as well as
reduced cell mediated immune surveillance, provides the ideal environment for a mutant cell to
evolve through the six or more minimum changes required for metastatic cancer to develop. These
features help both initiation and promotion resulting in a tumour that tries to replicate this
favourable environment by secreting angiogenetic and immunosuppressive factors.
14
Chapter 1
If this state occurs for several years, then random mutations in the cells of
the affected tissues, caused by carcinogens or unregulated proliferation,
would occur not only in an immunologically tolerant, but also a microvesselrich environment. Phenotypic changes, e.g. proteins resulting from mutations
in the ras oncogene, which would normally be detected by cytotoxic
lymphocytes, may escape immune surveillance. At the same time, these cells
would have an adequate supply of oxygen and nutrients as well as clearance
of waste metabolic products allowing another step in the stochastic
progression towards malignancy to occur (Gjertsen et al, 1997). Indeed, it is
so important to maintain this environment that developing neoplastic cell
clones evolve to mimic this state in order to progress and metastasise. This
contention is supported by the fact that tumours secrete CMI
immunosuppressive cytokines such as TGpp and IL-10 (Kiessling et a/.,
2000).
Again, induction of COX-2 may be central to the development of an
angiogenic environment in many of the conditions leading to the subsequent
development of malignancy. COX-2 expressing tumour cells are associated
with the production of a number of angiogenic growth factors and the
synthesis and activation of matrix metalloproteinases (MMPs), both of
which favour tumour invasion and angiogenesis (Tsujii et al., 1997; Tsujii et
a/., 1998; Takahashi et al., 1999). Cigarette smoke carcinogens, including
the tobacco-specific carcinogen NNK (which reproducibly induces
pulmonary adenocarcinomas in laboratory rodents) and nicotine are
associated with COX-2 upregulation. NNK, which is a beta-adrenergic
receptor agonist, does so by releasing arachidonate and nicotine acts through
nicotinic acetylcholine receptors (Saareks et al, 1998). Inhibition of COX-2
activity reduces IL-6 and IL-8 levels secreted by human cell lines further
supporting the strong link between inflammation, HI cytokine expression
and angiogenesis (Luca et al, 1997; Salgado et al, 1999; Hong et al, 2000).
6.
INFLAMMATION AND APOPTOSIS
Chronic inflammation also gives rise to the production of growth factors
and cytokines, and the activation of intracellular cell survival pathways that
would result in inhibition of apoptosis. An example of such a factor released
during inflammatory states is macrophage inhibitory factor (MIF), which has
recently been shown to repress the transcription activity of p53 and its
downstream targets p21 and bax, thereby having a marked anti-apoptotic
effect (Cordon-Cardo and Prives, 1999; Hudson et al., 1999). Experimental
evidence indicates that p53 plays an important role in the mediation of Th-1
cytokine-induced cytotoxicity (Yeung and Lau, 1998; Das et al., 1999; Kano
et al, 1999; Um et al., 2000; Takagi et al., 2000). p53 induces Transporter
Associated with Antigen Processing (TAP) 1 expression through a p53-
7. Inflammation and Cancer
15
responsive element. TAPl is required for the MHC class I antigen
presentation pathway. p73, which is homologous to p53, also induces TAPl
and cooperates with p53 to activate TAPl. Through the induction of TAPl,
p53 enhances the transport of MHC class I peptides and expression of
surface MHC-peptide complexes. p53 cooperates with IFN-y to activate the
MHC class I pathway. These results indicate that, as part of their function as
tumour suppressors, p53 and its homologue p73 may play a role in tumour
surveillance (Zhu et al, 1999). Therefore, inflammation is capable of
inactivating one of the most important cell regulatory pathways controlling
cancer development, reducing the effectiveness of the body's own cellular
defense reaction to a mutation. p53 also has a key role in the regulation of
angiogenesis, in part through induction of the anti-angiogenic factor
thrombospondin (Dameron, 1994). Furthermore, mutations of p53 may result
in induction of the synthesis of the most potent angiogenic agent known,
VEGF, leading to increased angiogenesis (Kieser et aL, 1994; Volpert et al,
1997). Therefore, loss of p53 would also result in an impaired CMI response,
facilitate angiogenesis, and result in a loss of apoptotic activity. Mutations of
the ras oncogene can induce IL-8 and induce stromal inflammation that can
lead to cancer progression (Sparmann and Bar-Sagi, 2004).
There is thus increasing evidence that exposure to carcinogens, such as
ultraviolet light (UV) (Athar et al, 1989), the tobacco-specific carcinogen
NNK (El-Bayoumy et al, 1999), nicotine (Saareks et al, 1998),
Helicobacter pylori (Konturek et al, 2000; Sawaoka et al, 1998a) and
colonic luminal contents, in particular the dihydroxy bile acids deoxycholate
and chemodeoxycholate (Zhang et al, 2000; Glinhammar et al, 2001) all
upregulate COX-2 in the affected tissue. In both non-neoplastic and
neoplastic cells, COX-2 is associated with cell proliferation (Tsuji et al,
1996; McGinty et al, 2000) and inhibition of apoptosis, at least in part
through the induction of bcl-2 (Tsujii and DuBois, 1995).
The serine/threonine kinase Akt (protein kinase B) is activated in
response to a variety of stimuli. This factor provides a survival signal that
protects cells from apoptosis induced by growth factor withdrawal. Through
the phosphorylation of specific targets such as Bad (del Peso et al, 1997)
and procaspase-9 (Cardone et al, 1998), the Akt cell survival signalling
pathway inhibits apoptosis. Some carcinogens act, at least in part, by
inducing oxidative stress in exposed cells. Oxidative stress results in the
activation of intracellular survival cell signalling pathways. In a variety of
cell types, H2O2, an inducer of oxidative stress, has been shown to induce
elevated Akt activity in a time- and dose-dependent manner by a mechanism
involving phosphoinositide 3-kinase (PI3K). Inhibitors of PI3K activity,
including wortmannin and LY294002, and expression of a dominant
negative mutant of p85, a regulatory component of PI3K, inhibited H2O2